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Interface-induced polymerization strategy for constructing titanium dioxide embedded carbon porous framework with enhanced chemical immobilization towards lithium polysulfides
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作者 Yue Ouyang Xiaoxiao Li +9 位作者 Jiexin Zhu Wei Zong Yuhang Dai Xuan Gao Wei Zhang Shengyuan Yang roohollah bagherzadeh Feili Lai Yue-E Miao Tianxi Liu 《Nano Research》 SCIE EI CSCD 2024年第3期1473-1481,共9页
The shuttle effect induced by soluble lithium polysulfides(LiPSs)is known as one of the crucial issues that limit the practical applications of lithium-sulfur(Li-S)batteries.Herein,a titanium dioxide nanoparticle embe... The shuttle effect induced by soluble lithium polysulfides(LiPSs)is known as one of the crucial issues that limit the practical applications of lithium-sulfur(Li-S)batteries.Herein,a titanium dioxide nanoparticle embedded in nitrogen-doped porous carbon nanofiber(TiO_(2)@NCNF)composite is constructed via an interface-induced polymerization strategy to serve as an ideal sulfur host.Under the protection of the nanofiber walls,the uniformly dispersed TiO_(2) nanocrystalline can act as capturing centers to constantly immobilize LiPSs towards durable sulfur chemistry.Besides,the mesoporous microstructure in the fibrous framework endows the TiO_(2)@NCNF host with strong physical reservation for sulfur and LiPSs,sufficient pathways for electron/ion transfer,and excellent endurance for volume change.As expected,the sulfur-loaded TiO_(2)@NCNF composite electrode presents a fabulous rate performance and long cycle lifespan(capacity fading rate of 0.062%per cycle over 500 cycles)at 2.0 C.Furthermore,the assembled Li-S batteries harvest superb areal capacity and cycling stability even under high sulfur loading and lean electrolyte conditions. 展开更多
关键词 interface-induced polymerization electrospun porous nanofibers lithium-sulfur(Li-S)batteries high sulfur loading lithium polysulfides(LiPSs)immobilization
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具有自适应机械弹性的纳米纤维互锁多孔石墨烯复合气凝胶用于高度可逆的无枝晶锂金属负极
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作者 冯之欣 莫璐璐 +9 位作者 陈开 钱雨姗 张镭骞 杨升元 roohollah bagherzadeh 赖飞立 樊玮 张超 缪月娥 刘天西 《Science China Materials》 SCIE EI CAS CSCD 2023年第8期3065-3074,共10页
具有最高理论容量的锂金属被认为是下一代高能量密度电池中最有前景的负极,但长循环过程中的锂枝晶生长和负极的体积膨胀阻碍着其实际应用.尽管已有研究使用石墨烯气凝胶等三维主体用于容纳锂金属,但单一的石墨烯气凝胶难以承受充放电... 具有最高理论容量的锂金属被认为是下一代高能量密度电池中最有前景的负极,但长循环过程中的锂枝晶生长和负极的体积膨胀阻碍着其实际应用.尽管已有研究使用石墨烯气凝胶等三维主体用于容纳锂金属,但单一的石墨烯气凝胶难以承受充放电过程中负极的大体积变化.因此,本文制备了具有自适应机械弹性的聚酰亚胺纳米纤维互锁多孔石墨烯复合气凝胶(PI-HGCA),将其作为复合主体结构用于容纳锂金属.具有面内纳米孔的多孔石墨烯纳米片可以有效地调节锂离子通量并提供高度定向的离子转移路径.此外,三维复合气凝胶主体由水平排列的多孔石墨烯片层和互锁的聚酰亚胺纳米纤维构成,其在长期循环过程中对负极的体积变化表现出高度可逆的自适应压缩弹性.预锂化的PI-HGCA负极在对称电池中显示出极低的过电势(46 mV),并具有1300次的长循环寿命;其与LiFePO_(4)正极所组装而成的全电池在1 C下经过800次循环后仍然显示出81.2%的超高容量保持率,表明该互锁气凝胶复合结构在高能量密度锂金属电池中具有巨大应用潜力. 展开更多
关键词 长循环寿命 水平排列 理论容量 复合气凝胶 高能量密度 石墨烯纳米片 聚酰亚胺 复合结构
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